Graham Field Hausted 5E82EYEST User manual

HP_5E82-INS-LAB-RevA23
ELECTRIC SURGI-STRETCHER
5E82EYEST, 5E82EYXST, 5B800ST
ELECTRIC SURGI-STRETCHER WITH
NAVIGATOR SMARTDRIVE SYSTEM
5E82EYEST-PD, 5E82EYXST-PD, 5B800ST-PD
OPERATING MANUAL
SAVE THIS MANUAL FOR FUTURE USE.

CONTENTS
INTRODUCTION — A WORD FROM GF HEALTH PRODUCTS, INC. ............................................................................................ 4
INDICATIONS FOR USE ........................................................................................................................................................... 4
SERVICE INFORMATION ......................................................................................................................................................... 4
ADVISORY................................................................................................................................................................................. 4
1 LIST OF WARNINGS AND CAUTIONS............................................................................................................................................. 5
SIGNIFICANCE OF SAFETY STATEMENTS .................................................................................................................................... 5
DANGER / WARNING / CAUTION / NOTICE SUMMARY ...................................................................................................... 5
DANGER: TO REDUCE THE RISK OF BURNS, FIRE, OR ELECTRIC SHOCK ........................................................ 5
WARNING: TO REDUCE THE RISK OF PERSONAL INJURY .................................................................................... 5
WARNING — CAUTIONS AND PROPER OPERATION ................................................................................................................... 6
ELECTROMAGNETIC COMPATIBILITY (EMC) INFORMATION ..................................................................................................... 7
IDENTIFICATION LABEL................................................................................................................................................................... 7
2 UNCRATING INSTRUCTIONS .......................................................................................................................................................... 8
IMPORTANT — REPORT ANY SHIPPING DAMAGE IMMEDIATELY: ............................................................................................ 8
NOTICE — POSSIBLE EQUIPMENT DAMAGE: .............................................................................................................................. 8
WARNING — PERSONAL INJURY HAZARD:.................................................................................................................................. 8
ENVIRONMENTAL CONDITIONS .................................................................................................................................................... 8
OPERATING .............................................................................................................................................................................. 8
STORAGE AND TRANSPORT.................................................................................................................................................. 8
UNPACKING INSTRUCTIONS .......................................................................................................................................................... 8
3 OPERATING INSTRUCTIONS........................................................................................................................................................... 9
3.1 SURGI-STRETCHER SPECIFICATIONS.................................................................................................................................. 9
ELECTRICAL SPECIFICATIONS.............................................................................................................................................. 9
3.2 FEATURES, WARNINGS AND PROPER OPERATION OPERATING INSTRUCTIONS ....................................................... 10
WARNINGS — CAUTIONS AND PROPER OPERATION ...................................................................................................... 10
FEATURES .............................................................................................................................................................................. 11
3.3 BRAKING AND STEERING OPERATION WITH SMART CASTER TECHNOLOGY ............................................................ 12
3.3.1 APPLYING THE BRAKES............................................................................................................................................ 12
3.3.2 UNLOCKING THE BRAKES........................................................................................................................................ 12
3.3.3 ACTIVATING ADVANCED STEER MODE — PENDANT ................................................................................................13
3.3.4 ACTIVATING ADVANCED STEER MODE – MANUALLY ...............................................................................................13
3.3.5 DEACTIVATING ADVANCED STEER MODE — PENDANT....................................................................................... 14
3.3.6 DEACTIVATING ADVANCED STEER MODE – MANUALLY ...................................................................................... 14
CASTER PEDAL POSITIONS...................................................................................................................................... 14
3.4 ELECTRIC CONTROL LOCATIONS....................................................................................................................................... 15
3.4.1 PENDANT CONTROL STORAGE LOCATION............................................................................................................ 15
3.4.2 PLUG LOCATION ........................................................................................................................................................ 15
3.4.3 LOW BATTERY ALARM .............................................................................................................................................. 15
3.4.4 FOOT CONTROL ......................................................................................................................................................... 15
3.5 HEIGHT AND PATIENT SURFACE ADJUSTMENT ............................................................................................................... 16
3.5.1 LOCK / UNLOCK (BUTTON 1).................................................................................................................................... 16
3.5.2 HEIGHT (HI / LO) (BUTTONS 2 AND 9)...................................................................................................................... 16
3.5.3 BACK SECTION UP / DOWN (BUTTONS 3 AND 10) ................................................................................................ 17
3.5.4 KNEE FLEX UP / DOWN (BUTTONS 4 AND 11)........................................................................................................ 17
3.5.5 AUTO CONTOURING UP / DOWN (BUTTONS 5 AND 12)........................................................................................ 18
3.5.6 BRAKE AND STEER MODE OPERATION (BUTTONS 6 AND 13) ............................................................................ 18
3.5.7 TRENDELENBURG, SUPINE AND REVERSE TRENDELENBURG POSITIONS (BUTTONS 7, 14 AND 20).......... 19
3.5.8 MEMORY AND PRESET FUNCTIONS (BUTTONS 15-18) ........................................................................................ 20
3.5.9 BATTERY (BUTTON 19) .............................................................................................................................................. 21
3.5.10 HOME (BUTTON 8)...................................................................................................................................................... 21
3.5.11 EMERGENCY DROP BACK........................................................................................................................................ 21
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3.6 HEADREST.............................................................................................................................................................................. 22
3.6.1 ADJUSTING THE HEADREST .................................................................................................................................... 22
3.7 COMMON OPTIONAL ACCESSORIES ................................................................................................................................. 23
3.7.1 MOUNTING THE WRIST REST .................................................................................................................................. 23
3.7.2 ADJUSTING THE WRIST REST.................................................................................................................................. 23
3.8 PUSH HANDLES..................................................................................................................................................................... 24
3.8.1 OPERATING THE PUSH HANDLES ........................................................................................................................... 24
ROTATING AND POSITIONING THE HAND GRIPS .................................................................................................. 24
OPERATING THE PUSH HANDLES WITH THE BACK IN RAISED POSITION ........................................................ 24
OPERATING THE PUSH HANDLES WITH THE BACK IN LOWERED POSITION ................................................... 24
3.9 PERMANENTLY MOUNTED IV ROD OPERATION (ALL MODELS) ..................................................................................... 25
3.9.1 PUTTING IV ROD IN UP POSITION ........................................................................................................................... 25
3.9.2 EXTENDING IV ROD ................................................................................................................................................... 25
3.9.3 RETRACTING IV ROD................................................................................................................................................. 25
3.10 PATIENT RAIL OPERATION (ALL MODELS)......................................................................................................................... 26
3.10.1 RAISING THE RAIL ..................................................................................................................................................... 26
3.10.2 HALF HEIGHT.............................................................................................................................................................. 26
3.10.3 LOWERING THE RAIL................................................................................................................................................. 26
4 TROUBLESHOOTING GUIDE......................................................................................................................................................... 27
4.1 ELECTRIC POWERED STRETCHERS................................................................................................................................... 27
4.2 BATTERY REPLACEMENT..................................................................................................................................................... 27
5 PREVENTIVE MAINTENANCE FOR THE USER ............................................................................................................................ 29
6 OPTIONAL ACCESSORIES ............................................................................................................................................................ 30
7 GF HEALTH PRODUCTS, INC. LIMITED WARRANTY FOR HAUSTED BRAND STRETCHERS AND CHAIRS ....................... 31
8 DISPOSAL AND KEY TO SYMBOLS.............................................................................................................................................. 32
DISPOSAL........................................................................................................................................................................................ 32
KEY TO SYMBOLS.......................................................................................................................................................................... 32
9 APPENDIX ........................................................................................................................................................................................ 33
9.1 GUIDANCE AND MANUFACTURER’S DECLARATION — ELECTROMAGNETIC EMISSIONS ........................................ 33
9.2 ENCLOSURE PORT 1 .............................................................................................................................................................. 34
9.3 ENCLOSURE PORT IMMUNITY TO RF WIRELESS COMMUNICATIONS EQUIPMENT 1 ................................................. 34
9.4 INPUT AC POWER PORT 1 ..................................................................................................................................................... 35
9.5 PATIENT COUPLING PORT 1.................................................................................................................................................. 36
9.6 SIGNAL INPUT/OUTPUT PARTS PORT 1 .............................................................................................................................. 37
9.7 RECOMMENDED SEPARATION DISTANCES BETWEEN PORTABLE AND MOBILE RF COMMUNICATIONS
EQUIPMENT AND HAUSTED STRETCHERS ....................................................................................................................... 38
9.8 NOTES TO SECTION 9........................................................................................................................................................... 38
10 5E82 / 5B800-PD NAVIGATOR SMARTDRIVE SYSTEM (“NSD”) ADDENDUM .......................................................................... 39
COPYING PROHIBITED
This manual is protected by Federal Copyright Law, which provides for damages of up to USD
$20,000, as well as criminal nes and imprisonment, for unauthorized copying.
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INTRODUCTION — A WORD FROM GF HEALTH PRODUCTS, INC.
This manual contains important information on proper use and maintenance of the Hausted®
Series 5E82 / 5B8 Surgi-Stretchers. All personnel involved in the use and maintenance of this
equipment must carefully review and comply with the warnings, cautions and instructions
contained in this manual. These instructions are important to protect the health and safety of
personnel operating these models and should be retained in a conveniently accessible area for
quick reference.
Complete instructions for uncrating and putting your new equipment in service, as well as
equipment drawings, have been furnished. If missing, contact GF Health Products, Inc. (“GF”) for
replacement copies, giving the serial number and model number of the unit.
GF Health Products, Inc. carries a complete line of accessories for use with these stretchers; your
representative will gladly review these with you.
Indications for Use
The Hausted Surgi-Stretchers are intended for a healthcare professional to use in patient treatment,
transport, or recovery. This product has an expected service life of ve years.
The articulating head piece with dual operating control knobs allows adjustability and precise
movement of the head section. Patient positioning is convenient and easy for both care provider and
patient with the electric/battery powered controls for adjustment of height, backrest and knee ex.
To ensure the basic safety of the patient, the stretcher is designed, tested, and evaluated to IEC
Standard 60601-1 and in accordance with IEC 60601-2-46 wherein the essential performance in
any single fault or combined fault condition is no unwanted movement of the stretcher when in
use. See also page 7 Electromagnetic Compatibility (EMC) information. The stretcher is tested and
certied to IEC 60601-1-2 (Ed. 4) for EMC.
Service Information
A thorough preventive maintenance program is essential to safe and proper unit operation. This
manual contains maintenance schedules and procedures which should be followed for satisfactory
equipment performance.
We encourage you to contact GF Health Products, Inc. with maintenance concerns.
Advisory
A listing of the safety precautions to be observed when operating and servicing this equipment
can be found in Section 1 of this manual. Do not operate or service the equipment until you have
become familiar with this information. Any alteration of this equipment not authorized or performed
by GF Health Products, Inc., could aect its operation, will void the warranty, could violate national,
state, and local regulations, and could jeopardize your insurance coverage.
Info: Column 1 below applies only if product was purchased outside the U.S.
EC REP
EC Authorized Representative:
CEpartner4U BV
ESDOORNLAAN 13
3951DB MAARN
The Netherlands
[phone]
Manufactured by:
GF Health Products, Inc.
One Graham-Field Way
Atlanta GA 30340-3140
1.770.368.4700 Main
1.770.368.2386 Fax
www.grahameld.com
www.Hausted.com
Class 1 Equipment
Type B Equipment
Equipment not suitable for use
in the presence of ammable
anesthetic mixture with air or
oxygen or nitrous oxide.
IPX4 Not suitable for continuous
operation (Duty Cycle:
10% 2 Min. in 18 Min.)
Info: The base language of this document is ENGLISH. Any translations must be made from the base language document.
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1 LIST OF WARNINGS AND CAUTIONS
IMPORTANT: Before using the Surgi-Stretcher, please read and adhere to the following
safety precautions and warnings. Failure to do so could result in serious personal injury or
damage to the Stretcher.
Always consult your healthcare professional to determine safe methods most suitable for your
individual abilities. Protect yourself, your attendant, and the Surgi-Stretcher by having it serviced
regularly. If you experience any malfunction, contact your Graham-Field authorized distributor
immediately, as a hazardous condition could result, causing personal injury or damage to the
Stretcher.
Periodic inspection, adjustment and replacement of worn parts are necessary to provide years of
excellent service. Maintenance MUST be performed by qualied personnel ONLY.
SAVE THESE INSTRUCTIONS.
SIGNIFICANCE OF SAFETY STATEMENTS
Please note the following special statements, used throughout this manual, and their signicance:
DANGER: Indicates a potential hazard situation or unsafe practice that, if not avoided, will
result in death or serious personal injury.
WARNING: Indicates a potential hazard situation or unsafe practice that, if not avoided,
could result in death or serious personal injury.
CAUTION: Indicates a potential hazard situation or unsafe practice that, if not avoided,
could result in minor or moderate personal injury.
sNOTICE: Indicates a potential hazard situation or unsafe practice that, if not avoided, could
result in product or property damage.
Info: Provides application recommendations or other useful information to ensure that
you get the most from your product.
DANGER / WARNING / CAUTION / NOTICE Summary
The following is a listing of the safety precautions which must be observed when operating and
servicing this equipment. These precautions are repeated (in whole or in part), where applicable,
throughout the manual.
DANGER: To Reduce the Risk of Burns, Fire, or Electric Shock
DANGER: SHOCK HAZARD — To reduce the risk of electric shock, unit is to be serviced by
qualied personnel only.
DANGER: SHOCK HAZARD — To avoid the risk of electric shock, this equipment must only
be connected to supply mains with protective earth.
WARNING: To Reduce the Risk of Personal Injury
WARNING: LACERATION HAZARD — When cutting bands always use a tool specically
designed for that purpose. This will help to avoid personal injuries frequently incurred when
bands are cut and tension released.
WARNING: Do not sit on end — tipping may occur.
WARNING: Ensure IV rod is inserted completely into socket up to the arrow before applying
load.
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WARNING — CAUTIONS AND PROPER OPERATION
WARNING: The Series 5E82 / 5B800 stretchers have a maximum patient weight capacity of
800 lb (363 kg), EVENLY DISTRIBUTED.
WARNING: The Series 5E82 / 5B800 stretchers have a maximum weight, including
equipment weight, and patient weight of 1200 lb (544 kg), EVENLY DISTRIBUTED.
WARNING: Patient entry, egress and transfer should always be performed with the brakes
locked.
WARNING: The patient transport position is pushing from the patient head end in the supine
position.
WARNING: The brakes should always be locked and patient side rails up when patient is
not in transport.
WARNING: Clip patient pendant to rail when not in use – keep cord clear of moving parts.
WARNING: All electric powered stretchers are equipped with a built-in battery backup
system, but the unit should remain plugged into wall receptacle during normal use. The
battery backup is intended for transport and EMERGENCY only.
WARNING: The stretcher has a warning label on both the head and foot end stating: “Do
not sit on end - as tipping may occur.”
WARNING: Patient entry, egress, and transfer from the stretcher should always be from the
center side rail location with the side rail in the down position and brakes locked.
WARNING: The back quick drop handle is intended to be used during emergency situations
only.
WARNING: To turn on electric controls, plug into wall receptacle. To turn off, remove plug
from wall receptacle. Electric powered stretchers do not have a separate on / off switch.
WARNING: Always disconnect the power source whenever troubleshooting or servicing any
electric powered stretcher.
WARNING: Cables can become pinched. Keep cables away from column.
WARNING: Steam cleaning and pressure washing of chair is not recommended and can
void warranty.
WARNING: Do not modify the equipment without the authorization of the manufacturer.
WARNING: When lowering the rails, ensure patient and caregiver body and extremities are
clear of pinch points before operating the rail.
WARNING: Keep hands clear of pinch points.
WARNING: Stow away power cord when not in use to prevent injury or damage.
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ELECTROMAGNETIC COMPATIBILITY (EMC) INFORMATION
WARNING: Medical Electrical Equipment needs special precautions regarding EMC and
needs to be installed and put into service according to the EMC information provided in this
manual.
WARNING: Electronic equipment may be inuenced by Radio Frequency (RFI). Caution
should be exercised with regard to the use of portable communications in the area around
such equipment. Portable RF communications equipment (including peripherals such as
antenna cables and external antennas) should be used no closer than 12 inches (30 cm)
to any part of the Hausted equipment including specied Hausted equipment cables.
Degradation of the performance of the Hausted equipment could result.
WARNING: If RFI causes erratic behavior, unplug the electric Hausted equipment
immediately. Leave unplugged while transmission is in progress.
WARNING: The use of accessories, transducers, and cables other than those specied by
the manufacturer may result in increased emissions or decreased immunity of the Hausted
equipment. GF cables and accessories include motor cables, mains cable, pendant cables,
and back up battery and cable.
WARNING: This equipment should not be used adjacent to or stacked with other
equipment. If adjacent or stacked use with other equipment is necessary, this Hausted
equipment and the other equipment should be observed to verify that they are operating
normally.
WARNING: The EMISSIONS characteristics of this equipment make it suitable for use in
industrial areas and hospitals (CISPR 11 class A). If it is used in a residential environment
(for which CISPR 11 class B is usually required) this equipment might not offer adequate
protection to radio frequency communication services. The user might need to take
mitigation measures, such as relocating or reorienting the equipment.
identification label
Identification label location Identification label example
model
serial number
The stretcher identication label identies the stretcher serial number and model, essential
information when ordering replacement parts or claiming parts under warranty. The identication
label, shown above, is beneath the patient left surface at midpoint of frame. Have this information
ready when calling our Customer Service or Technical Support sta at 1.770.368.4700; it will allow
us to better assist you and quickly answer your questions and concerns.
IDENTIFICATION LABEL
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2 UNCRATING INSTRUCTIONS
IMPORTANT — REPORT ANY SHIPPING DAMAGE IMMEDIATELY:
WARNING:Inform shipper of any damage — leave carton intact. Leave equipment in the
receiving area until inspection is complete.
NOTICE — POSSIBLE EQUIPMENT DAMAGE:
sNOTICE: The crate contains fragile, expensive medical equipment. Uncrate and handle
carefully. If after uncrating the equipment you nd any damage (no matter how slight),
report the damage to GF Health Products, Inc.
WARNING — PERSONAL INJURY HAZARD:
WARNING:When cutting bands, always use tool specically designed for that purpose.
This will help avoid personal injuries possibly incurred when bands are cut and tension is
released.
ENVIRONMENTAL CONDITIONS
Operating
Temperature 5°C to 40°C
Relative Humidity 20% to 90% @ 86°F
(30°C)
Atmospheric Pressure 700 to 1060 hPa
Storage and Transport
Temperature -10°C to 50°C
Relative Humidity 20% to 90% @ 86°F
(30°C)
Atmospheric Pressure 700 to 1060 hPa
UNPACKING INSTRUCTIONS
IMPORTANT: Follow each step in the order shown in these instructions.
Your Hausted equipment has been carefully packed at our manufacturing plant to ensure safe
shipment to your medical facility. There are several procedures you must follow to put your new
equipment in service. These procedures only take a few minutes to complete and all are required
to ensure proper operation of the equipment.
1. Cut the two bands around the shipping carton.
2. Remove the top half of the carton and cut one side of the bottom half.
3. Remove the equipment from the carton.
4. Check to see if all features of the equipment work properly. If all the features work, advance to
step 5. If any features do not work properly, call GF Health Products, Inc. at 1.770.368.4700.
Info: Plug the unit into a wall socket prior to checking any electric features. The battery
will reach full charge after approximately 10 hours.
5. Clean the equipment using mild detergent to remove any dirt accumulated during shipment,
and place the equipment into service.
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3 OPERATING INSTRUCTIONS
3.1 SURGI-STRETCHER SPECIFICATIONS
Info: All dimensions, unless otherwise specified, are in inches and ±.375 (1 cm).
GF Health Products, Inc. reserves the right to change specifications without notice.
Model Standard Width
5E82EYEST &
5E82EYEST-PD
Wide Width
5E82EYXST &
5E82EYXST-PD
Bariatric
5B800ST & 5B800ST-PD
Height Range: High
40 in. ±1 in. [101 cm ±2.5 cm]
Height Range: Low
22 in. ±1 in. [55.8 cm] ±2.5 cm
Overall Width
32 in. [81 cm] 37 in. [94 cm] 37 in. [94 cm]
Overall Length
92.35 in. [234.6 cm] 88.38 in. [224.3 cm]
Patient Surface Width
25 in. [64 cm] 30 in. [76 cm]
Patient Surface Length
85.38 in. [224.3 cm] 80.25 in. [203.8 cm]
Backrest
Degree of Movement
0° - 90°
Knee Flex
Degree of Movement
0° - 60°
Trendelenburg / Reverse
Trendelenburg
15° ±2°
Retracto Rail Height
14 in. [36 cm]
Retracto Rail Length
49 in. [125 cm] 63 in. [160 cm]
Casters
5.9 in. [15 cm] Electric Lock / Steer
Maximum Weight Capacity
(EVENLY DISTRIBUTED)
800 lb [363 kg]
Applied Parts:
Pads, Linens, Side Rails, Some Accessories
Mattress Pad Thickness
3 in. [7 cm] 5 in. [13 cm]
Electrical Specications
Product Classication:
1
Input Voltage:
100V - 240V ~ 50/60 Hz
Amperage:
Max. 4.0A
Duty Cycle:
10% (2 Min. in 18 Min.)
IP Rating:
IPX4 All Models
Grounding Protection:
Type B
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Tipping (Both Ends)
See Warning, A
3-Position Side Rails
See Warnings, C, H, & I
Pinch Points
(Both Ends)
See Warning, L
Power to Stretcher
See Warnings, J, K, & M
Fowler Backrest
Quick-Drop Handle
See Warning, G
Weight Capacity
(Back)
See Warning, B
Pinch Points
(Both Sides)
See Warning, L
3.2 FEATURES, WARNINGS AND PROPER OPERATION OPERATING INSTRUCTIONS
WARNINGS — CAUTIONS AND PROPER OPERATION (See Diagram Below)
A. WARNING: Do not sit on end — tipping may occur.
B. WARNING: The stretchers have a warning label located at the head and foot end stating: Maximum
patient weight 800 lb (363 kg) for 5E82 and 5B800 models.
C. WARNING: Patient entry, egress and transfer should always be done with the brakes locked.
D. WARNING: The brakes should always be locked and patient side rails up when patient is not in
transport.
E. WARNING: The patient pendant has a warning label stating: Clip pendant to rail when not in use —
keep cord clear of moving parts. As is stated on the cable adjacent to the pendant.
F. WARNING: All electric stretchers are equipped with a built-in battery backup system,
but it is recommended that the unit remain plugged into wall receptacle during normal use. The
battery backup is recommended for transport and EMERGENCY only.
G. WARNING: The Fowler backrest quick-drop handle is intended to be used to lower patient during
EMERGENCY situations only.
H. WARNING: Ensure rail is locked before leaving patient.
I. WARNING: When lowering the rails, ensure patient and caregiver (or attendant) body and extremities
are clear of pinch points before operating the rail.
J. WARNING: To turn on electric controls, plug into wall receptacle; to turn off, remove plug from wall
receptacle. The electric powered stretchers do not have a separate on / off switch.
K. WARNING: Always disconnect the power source whenever servicing any electric powered stretcher.
L. WARNING: Keep hands clear of pinch points.
M. WARNING: Stow away power cord when not in use to prevent injury or damage.
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Features (Shown in Illustration of 5E82EYST and 5E82EYEST-PD below)
MIN HEIGHT
BACKREST
OVERALL LENGTH
NAVIGATOR
SMARTDRIVE
SYSTEM
ELECTRIC BASE
STORAGE
CASTERS
RAIL
PENDANT CONTROL
COLLAPSIBLE
IV POLE
MANUAL OVERRIDE
CASTER PEDALS
EMERGENCY BACKREST RETRACTABLE
PUSH HANDLES
ADJUSTABLE
HEADREST
NAVIGATOR
SMARTDRIVE
ENTIRE PERIMETER
PROTECTIVE
BUMPER SYSTEM
OVERALL LENGTH
PATIENT BELONGING
BAG HOOKS
COLLAPSIBLE
PUSH HANDLES
HOSPITAL GRADE PLUG
WARNINGS — CAUTIONS AND PROPER OPERATION (See List on Previous Page)
MIN HEIGHT
OVERALL LENGTH
BACKREST
NAVIGATOR
SMARTDRIVE
SYSTEM
ELECTRIC BASE
STORAGE
CASTERS
RAIL
PENDANT CONTROL
COLLAPSIBLE
IV POLE
MANUAL OVERRIDE
CASTER PEDALS
EMERGENCY BACKREST
RETRACTABLE
PUSH HANDLES
NAVIGATOR
SMARTDRIVE
ENTIRE PERIMETER
PROTECTIVE
BUMPER SYSTEM
OVERALL WIDTH
PATIENT BELONGING
BAG HOOKS
COLLAPSIBLE
PUSH HANDLES
HOSPITAL GRADE PLUG
Features (Shown in Illustration of 5B800ST & 5B800ST-PD below)
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Features (Shown in Illustration of 5E82EXYST and 5E82EXYEST-PD below)
MIN HEIGHT
BACKREST
OVERALL LENGTH
NAVIGATOR
SMARTDRIVE
SYSTEM
ELECTRIC BASE STORAGE
CASTERS
RAIL
PENDANT CONTROL
COLLAPSIBLE
IV POLE
MANUAL OVERRIDE
CASTER PEDALS
EMERGENCY BACKREST
RETRACTABLE
PUSH HANDLES
ADJUSTABLE
HEADREST
NAVIGATOR
SMARTDRIVE
ENTIRE PERIMETER
PROTECTIVE
BUMPER SYSTEM
OVERALL WIDTH
PATIENT BELONGING
BAG HOOKS
COLLAPSIBLE
PUSH HANDLES
HOSPITAL GRADE PLUG
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Figure 3.3-2
Figure 3.3-1
Figure 3.3-3
Figure 3.3-4
3.3 BRAKING AND STEERING
OPERATION WITH SMART CASTER
TECHNOLOGY
3.3.1 Applying the Brakes
To apply the four wheel central braking
system with the pendant, press the pendant
Brake On / O button; the LED above the
button then illuminates green (Figure 3.3-1),
and the blue caster pedals on all four corners
of the stretcher automatically lower to lock
(Figure 3.3-2), and all four caster wheels will then
be locked from swiveling and rotating.
Info: To prevent unintended movement, the
brakes engage automatically after the unit
has been stationary for 30 seconds.
To apply the four-wheel central braking system
manually, gently depress the blue caster pedal
at any of the four corners of the stretcher until
the pedal stops (Figure 3.3-2). The remaining
three pedals will then automatically lower to
lock (Figure 3.3-2), and all four caster wheels will
then be locked from swiveling and rotating.
sNOTICE: DO NOT apply excessive force to
pedal when manually applying brakes.
3.3.2 Unlocking the Brakes
To unlock the brakes with the pendant, press
the pendant Brake On / O button; the LED
above the button then goes out (Figure 3.3-3),
the blue caster pedals on all four corners of the
stretcher will then automatically rise to unlock
(Figure 3.3-4), and all four caster wheels will then
rotate and swivel freely.
To unlock the brakes manually, gently lift the
blue caster pedal at any of the four corners of
the stretcher until the pedal is in a horizontal
position (Figure 3.3-4); the remaining three
pedals will then automatically rise to unlock and
all four caster wheels will then rotate and swivel
freely.
WARNING: Ensure the brakes are locked
when the patient is not being transported.
sNOTICE: DO NOT apply excessive force to
pedal when manually unlocking brakes.
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3.3.3 Activating Advanced Steer Mode — Pendant
To activate Advanced Steer Mode with the pendant,
press the pendant Steer Mode On / O button.
The LED above the button then illuminates green
(Figure 3.3-5), and the blue caster pedals automatically
rise (Figure 3.3-6) at the patient foot end of the stretcher.
All four caster brakes will unlock and the stretcher will
be ready for transport. Push the stretcher forward or
backward — both front casters will lock into Steer-Lock
position, which is ideal for pushing the stretcher from
the patient head end. The stretcher will steer along a
straight path, maneuver corners, and change direction
with minimal eort.
Note: The steer mode function (both by pendant
or manual) is disabled for stretchers with the
Navigator SmartDrive System. Activation with
the pendant results in an audible beep. Manual
activation will immediately return to the neutral
position.
Info: The casters will lock into Steer-Lock position
when turned to 6 o’clock or 12 o’clock, with the
stretcher’s patient foot end being 12 o’clock.
Info: Depending upon how the casters are oriented
when they lock, they can lock into Steer-Lock
position while trailing (6 o’clock) or leading (12
o’clock). If the casters lock in opposite orientations,
steering may be more difficult.
Info: The pendant will only lock the foot end
casters into Steer-Lock position.
3.3.4 Activating Advanced Steer Mode – Manually
When pushing from the head end: Activate foot
end Advanced Steer Mode by lifting the blue pedal
upward on either head end caster until the pedal stops
(Figure 3.3-6). Both foot end pedals will then rise to lock
foot end casters into Steer-Lock position, the head end
pedals will return to neutral position (Figure 3.3-4), and the
LED above the pendant Steer Mode On / O button will
illuminate green (Figure 3.3-5).
Figure 3.3-5
Figure 3.3-6
Figure 3.3-4
When pushing from the foot end: Activate head end Advanced Steer Mode
by lifting the blue pedal upward on either foot end caster until the pedal
stops (Figure 3.3-6). Both head end pedals will then rise to lock the head end
casters into Steer-Lock position, the foot end pedals will return to neutral
position (Figure 3.3-4), and the LED above the pendant Steer Mode On / O
button will illuminate green (Figure 3.3-5).
Info: It is not possible to lock the head end casters into Steer-Lock
position with the pendant. This can only be done with the foot end manual
activation.
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3.3.5 Deactivating Advanced Steer Mode —
Pendant
To deactivate Advanced Steer Mode with the
pendant, press the pendant Steer Mode On / O
button. The LED above the button will go out
(Figure 3.3-7) and the blue caster pedals in
Steer-Lock position will automatically lower to neutral
position (Figure 3.3-4). All four casters will now rotate
and swivel freely.
Info: All four casters must be parallel to each
other in the 6 o’clock or 12 o’clock position to
be able to properly go into neutral position.
Failure to place casters in this orientation may
cause the Steer Mode On / Off button to not
deactivate Steer Mode.
3.3.6 Deactivating Advanced Steer Mode –
Manually
Depress the blue caster pedal down to the neutral
position (Figure 3.3-4) on either caster locked into
Steer-Lock position. All four casters will now rotate
and swivel freely. Depressing the blue pedal down
past neutral until it stops will apply all four caster
brakes (Figure 3.3-2), locking all four casters into
brake position.
Info: After thirty seconds of no movement,
Advanced Steer Mode automatically deactivates
and all four caster wheels lock into brake
position.
WARNING: To prevent unintended movement,
activate or deactivate Advanced Steer Mode only
while the stretcher is stopped.
Caster Pedal Positions
The table below shows the blue caster pedal in
all three positions.
CASTER PEDAL POSITIONS
Pedal Up Steer-Lock
Position
Pedal Horizontal Neutral Position
(Swivel)
Pedal Down Brake Position
(Locked)
Figure 3.3-7
Figure 3.3-4
Figure 3.3-2
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3.4 ELECTRIC CONTROL LOCATIONS
3.4.1 Pendant Control Storage Location
The pendant is located on the bumper rail on
either side of the stretcher (Figure 3.4-1).
sNOTICE: Place pendant on bumper rail
when not in use. Keep cord clear of
moving parts.
3.4.2 Plug Location
This stretcher is equipped with a battery
backup for transport but the unit should be
plugged into a wall receptacle when not in
transport. The plug is located on the patient
right side of the stretcher (Figure 3.4-2). Do
not position the unit so that it is di cult to
disconnect the plug.
WARNING: The 5E82 Surgi-Stretcher
is equipped with a built in battery backup
system: nevertheless, the unit should
remain plugged into wall receptacle
during normal use. The battery backup
is recommended for transport and
emergency only.
3.4.3 Low Battery Alarm
This stretcher is equipped with an audible and
visual low battery alarm. When the system
requires charging, a continuous beep will
sound during motor operation, the pendant
LED above the BATTERY button will illuminate
green, and the control box LED will illuminate
amber.
3.4.4 Foot Control
Large red circle indicates optional foot control
storage location (Figure 3.4-3). Small red circle
indicates foot control plug-in location (Figure
3.4.3), which can also be used as an alternate
pendant plug-in location.
Figure 3.4-1
Figure 3.4-2
Figure 3.4-3
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3.5 HEIGHT AND PATIENT SURFACE ADJUSTMENT
1
2
3
9
5
4
19
Figure 3.5-1
3.5.1 LOCK / UNLOCK (button 1)
1
LOCK Press and hold LOCK button (1) for three seconds to lock
all functions. After ve LED ashes, all four UP LED’s (2-5)
illuminate steady green, indicating they are now locked; an
audible signal also indicates when locked and beeps up to
three times until button is released.
UNLOCK Press and hold LOCK and BATTERY buttons (1 and 19)
for one second to unlock all functions. A quick LED ash
indicates they are now unlocked; an audible signal also
indicates when unlocked.
UNLOCK INDIVIDUAL
FUNCTION
(PATIENT MODE)
Press and hold LOCK button (1) and press each UP button
(2-5) to unlock each function individually. As each button
is released, its LED will go out, indicating that function is
unlocked.
3.5.2 HEIGHT (HI / LO) (buttons 2 and 9)
2 HEIGHT UP Press and hold HEIGHT button (2) until desired height is achieved.
LED illuminates steady green while pressed, goes out when
released.
9 HEIGHT DOWN Press and hold HEIGHT DOWN button (9) until desired height is
achieved. LED illuminates steady green while pressed, goes out
when released.
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3.5 HEIGHT AND PATIENT SURFACE ADJUSTMENT
3
10
4
11
Figure 3.5-2
3.5.3 BACK SECTION UP / DOWN (buttons 3 and 10)
3 BACK UP Press and hold BACK UP button (3) until desired position is
achieved. LED illuminates steady green while pressed, goes out
when released.
10 BACK DOWN Press and hold BACK DOWN button (10) until desired position is
achieved. LED illuminates steady green while pressed,
goes out when released.
3.5.4 KNEE FLEX UP / DOWN (buttons 4 and 11)
4 KNEE FLEX UP Press and hold KNEE FLEX UP button (4) until desired position is
achieved. LED illuminates steady green while pressed,
goes out when released.
11 KNEE FLEX
DOWN
Press and hold KNEE FLEX DOWN button (11) until desired
position is achieved. LED illuminates steady green while pressed,
goes out when released.
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3.5 HEIGHT AND PATIENT SURFACE ADJUSTMENT
5
12
6
13
Figure 3.5-3
3.5.5 AUTO CONTOURING UP / DOWN (buttons 5 and 12)
5 AUTO
CONTOURING
UP
Press and hold AUTO CONTOURING UP button (5) until desired
position is achieved. LED illuminates steady green while pressed,
goes out when released.
12 AUTO
CONTOURING
DOWN
Press and hold AUTO CONTOURING DOWN button (12) until
desired position is achieved. LED illuminates steady green while
pressed, goes out when released.
3.5.6 BRAKE and STEER MODE Operation (buttons 6 and 13)
6 BRAKE
Press BRAKE button (6) to toggle on / off. When brakes are locked
(on), LED illuminates steady green; when brakes are unlocked
(off), LED goes out. To prevent unintended movement, brakes
lock automatically after stretcher is stationary for 30 consecutive
seconds.
13 STEER MODE
Press STEER MODE button (13) to toggle on / off. When steer
mode is activated, LED illuminates steady green; when steer mode
is off, LED goes out.
Note: Steer mode is not operable when brake is activated.
Note: Steer mode is disabled on stretchers equipped with the
Navigator SmartDrive System.
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3.5 HEIGHT AND PATIENT SURFACE ADJUSTMENT
7
14
20
Figure 3.5-4A
3.5.7 TRENDELENBURG, SUPINE and REVERSE TRENDELENBURG Positions
(buttons 7, 14 and 20)
7TRENDELENBURG
Press and hold TRENDELENBURG button (7) until desired
position is achieved. Stretcher automatically lowers back and
leg sections, tilts backward, and adjusts height. No LED.
14 SUPINE
Press and hold SUPINE button (14) until desired position is
achieved. Stretcher automatically levels back and leg sections
and adjusts height. No LED.
20 REVERSE
TRENDELENBURG
Press and hold REVERSE TRENDELENBURG button (20) until
desired position is achieved. Stretcher automatically lowers
back and leg sections, tilts forward, and adjusts height. No LED.
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